ENST00000426263.10:c.358G>T
MANE Select
|
ENSP00000416293.2:p.Glu120Ter
|
|
ENST00000674765.1:c.358G>T
|
ENSP00000501811.1:p.Glu120Ter
|
|
ENST00000675112.1:n.381G>T
|
|
|
ENST00000676254.1:n.807G>T
|
|
|
ENST00000372500.4:c.262G>T
|
ENSP00000361578.4:p.Glu88Ter
|
|
ENST00000426263.7:c.358G>T
|
ENSP00000416293.2:p.Glu120Ter
|
|
ENST00000439722.2:c.237G>T
|
ENSP00000395521.2:n.237G>T
|
|
ENST00000475162.3:c.257G>T
|
|
|
ENST00000625233.2:n.566G>T
|
|
|
ENST00000630287.2:c.358G>T
|
ENSP00000486694.1:p.Glu120Ter
|
|
NM_006516.2:c.358G>T
|
NP_006507.2:p.Glu120Ter
|
|
NM_006516.3:c.358G>T
|
NP_006507.2:p.Glu120Ter
|
|
NM_006516.4:c.358G>T
MANE Select
|
NP_006507.2:p.Glu120Ter
|
|